Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sonya Zaor"'
Autor:
Yury Monczak, Lidia Kasprzak, Jean Latreille, Sonya Zaor, Rachel Laframboise, Bruno Maranda, Marc Tischkowitz, William D. Foulkes, Nora Wong, George Chong, Carole Richard, Mona Kay Wu, Jean Gekas, Carly Pouchet, Jonathan Jarry, Régen Drouin, Laura Palma, Jean-Sébastien Brunet
Publikováno v:
Familial Cancer. 10:659-665
This is an 11-year survey of molecular analysis of APC germline mutations for the province of Quebec done at the Molecular Pathology Unit of the Jewish General Hospital which offers genetic testing for hereditary forms of colorectal cancer for the wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a22900a4e7ca904ca8d42aadcba08dc8
https://doi.org/10.1007/s10689-011-9468-4
https://doi.org/10.1007/s10689-011-9468-4
Autor:
Jean Latreille, Philip H. Gordon, Isabelle Thiffault, Sonya Zaor, Nora Wong, Victoria Marcus, Laura Palma, Sebastian Winocour, Jonathan Jarry, Adrian Gologan, Régen Drouin, Yves Giguère, William D. Foulkes, Lidia Kasprzak, Bharati Bapat, Yury Monczak, Jeremy R. Jass, Polymnia Galiatsatos, George Chong, Marc Tischkowitz, Karlene Australie
Publikováno v:
Human Mutation. 30:E797-E812
Lynch syndrome is one of the most common autosomal dominantly inherited cancer syndromes. Mutations in MLH1, MSH2, MSH6, and PMS2 account for greater than 98% of reported mutations in Lynch syndrome families. It has been reported that large genomic d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac3ae3f96568b94984ab0362ca05ee6
https://doi.org/10.1002/humu.21056
https://doi.org/10.1002/humu.21056
Autor:
Benoit Panzini, Niki Boyd, Cathy Gilpin, Sam S. Yoon, Sonya Zaor, Daniel Fontaine, Sylviane Olschwang, Sarah M. Nikkel, Jane Green, Carla Oliveira, Maria Ana Redal, Daniel G. Coit, Gregory Y. Lauwers, Lori Van Manen, David G. Huntsman, Pardeep Kaurah, Debrah Wirtzfeld, Paul D.P. Pharoah, Wendy S. Rubinstein, Jennifer Stroop, Antonio Pizzuti, Alessandro De Luca, Andrée MacMillan, Janine Senz, James M. Ford, Bridget A. Fernandez, Marc S. Greenblatt, Steven Gallinger, Carlos A. Vaccaro, Robert M. Greenstein, Daniel C. Chung, Wendy McKinnon, Scott M. Weissman, Courtney Sebold, Mary Connolly-Wilson, Marc Tischkowitz, Henry T. Lynch, Gianpaolo Suriano, Nicki Chun, Dwight Yim
ContextHereditary diffuse gastric cancer is caused by germline mutations in the epithelial cadherin (CDH1) gene and is characterized by an increased risk for diffuse gastric cancer and lobular breast cancer.ObjectiveTo determine whether recurring ger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f732fdbdb7380430fbb258a8fb011312
http://hdl.handle.net/11573/366499
http://hdl.handle.net/11573/366499
